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Published in: Medical Oncology 1/2013

01-03-2013 | Original Paper

The expression of moesin in astrocytoma: correlation with pathologic grade and poor clinical outcome

Authors: Ming Wu, Ding-yang Liu, Xian-rui Yuan, Qing Liu, Xin-jun Jiang, Dun Yuan, Jun Huang, Xue-jun Li, Zhi-quan Yang

Published in: Medical Oncology | Issue 1/2013

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Abstract

Moesin, a member of the ERM family, acts as a linker between the actin cytoskeleton and the plasma membrane and plays a key role in the control of cell morphology, motility, adhesion and other processes of tumourigenesis. The expression pattern and clinical significance of moesin in astrocytoma remain unknown. In this study, we used RT-PCR to systematically investigate the expression of moesin in 49 astrocytomas of different pathological grade and 6 normal brain tissues. We found that the mRNA expression levels of moesin in astrocytomas were significantly higher in comparison with normal brain tissues. Furthermore, moesin up-regulation was correlated with pathological grade of astrocytomas. Subsequently, we tested 112 astrocytomas and 14 normal brain tissues by immunohistochemistry. Similar results were also confirmed. Univariate and multivariate survival analysis were used to determine the correlations of moesin expression with overall survival and progression-free survival. Our results showed the expression of moesin was strongly negatively correlated with the patient progression-free survival and overall survival. These results suggest moesin protein involved in the genesis and progression of astrocytomas and might be regarded as an independent predictor of poor prognosis.
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Metadata
Title
The expression of moesin in astrocytoma: correlation with pathologic grade and poor clinical outcome
Authors
Ming Wu
Ding-yang Liu
Xian-rui Yuan
Qing Liu
Xin-jun Jiang
Dun Yuan
Jun Huang
Xue-jun Li
Zhi-quan Yang
Publication date
01-03-2013
Publisher
Springer US
Published in
Medical Oncology / Issue 1/2013
Print ISSN: 1357-0560
Electronic ISSN: 1559-131X
DOI
https://doi.org/10.1007/s12032-012-0372-z

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